Evidence map›Paper›PMID 36303796›Full record

ArticleFrontiers in bioinformatics2021

A Mechanistic Site-Of-Action Model: A Tool for Informing Right Target, Right Compound, And Right Dose for Therapeutic Antagonistic Antibody Programs.

Georgi I Kapitanov, Jeffrey R Chabot, Jatin Narula, Mahua Roy, Hendrik Neubert, Joe Palandra, Vahid Farrokhi, Jay S Johnson, Robert Webster, Hannah M Jones

Abstract read
In one paragraph

Article in Frontiers in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Georgi I KapitanovBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.
Jeffrey R ChabotBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.
Jatin NarulaBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.
Mahua RoyBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.
Hendrik NeubertBioMedicine Design, Pfizer Worldwide R&D, Andover, MA, United States.
Joe PalandraBioMedicine Design, Pfizer Worldwide R&D, Andover, MA, United States.
Vahid FarrokhiBioMedicine Design, Pfizer Worldwide R&D, Andover, MA, United States.
Jay S JohnsonBioMedicine Design, Pfizer Worldwide R&D, Andover, MA, United States.
Robert WebsterBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.
Hannah M JonesBioMedicine Design, Pfizer Worldwide R&D, Cambridge, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative modeling is increasingly utilized in the drug discovery and development process, from the initial stages of target selection, through clinical studies. The modeling can provide guidance on three major questions-is this the right target, what are the right compound properties, and what is the right dose for moving the best possible candidate forward. In this manuscript, we present a site-of-action modeling framework which we apply to monoclonal antibodies against soluble targets. We give a comprehensive overview of how we construct the model and how we parametrize it and include several examples of how to apply this framework for answering the questions postulated above. The utilities and limitations of this approach are discussed.

Indexed as

LC-MSmodeling and simulationPKPDQSPsite of action

Identifiers

PMID36303796
PMCPMC9581070

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.